2020年山东省牛羊疫病报告及监测数据分析

为了解山东省牛羊疫病的流行及免疫现状,汇总2020年山东省牛羊疫病报告数据以及监测数据等信息,分析牛羊疫病的时间分布、空间分布及病种分布;结合监测情况,分析牛羊疫病的免疫状况和暴发风险。2020年山东省牛病以新生犊牛腹泻、牛病毒性腹泻和牛传染性鼻气管炎为主,突发输入性牛结节性皮肤病,羊病以沙门氏菌病、绵羊疥癣和布鲁氏菌病为主;牛病主要集中在鲁北和鲁西北地区,羊病主要集中在鲁中、鲁西、鲁南及半岛北部地区;牛羊疫病有一定的时间分布特征,7—9月份牛病暴发较频繁,6—9月和12月羊病发病率较高;口蹄疫、小反刍兽疫免疫水平较高,整体暴发风险可控,但仍存在一定的牛羊口蹄疫非结构蛋白抗体阳性;布鲁氏菌病免疫水平偏低,感染抗体阳性群体内个体感染情况较严重,羊群感染程度高于牛群。分析提示:鲁北和鲁西北地区应重点加强新生犊牛腹泻、牛病毒性腹泻等牛病的防控,鲁中、鲁西、鲁南及半岛北部地区应加强沙门氏菌病、布鲁氏菌病等羊病的防控,继续推进牛羊布鲁氏菌病净化场(县)创建工作;对口蹄疫和小反刍兽疫等防控效果较好的疫病以及新传入的牛结节性皮肤病,应持续加强免疫和监测,防止疫情传入或复发。     

羊沙门氏菌病流行与防治

羊沙门氏菌病是是由多种致病性沙门氏菌感染引发的一种急性传染性疾病,不同年龄品种的羊都可以受到病原侵染,其中对羔羊造成的危害最为严重,尤其是断奶不久后的羔羊感染沙门氏菌后,表现的临床症状最为明显,致死率最高。临床上由于致病性沙门氏菌的种类较多,侵染途径多样,一旦受到病原侵染,将很难清理,会造成羊群反复流行,带来的经济损失不可估量。该文主要探讨羊沙门氏菌病的流行特点与防治措施。     

前桥摆转转向式四驱底盘结构形状指数的优化

前桥摆转转向式四驱底盘可直接转入下一畦作业,提高了小地块工作行程率,在地头宽度小于等于1个作业宽度时,更有利于机耕过程中的转向操作。为此,通过ADAMS软件仿真,以最小地头宽度为目标对底盘结构参数进行了优化。仿真结果表明,底盘在作业过程中从一畦进入地头直接转入相邻的下一畦时,后内侧轮基本上不吃入上一畦,最小地头宽度与长宽比成反比。在底盘转向时行走轮不干涉后悬挂农具的前提下,底盘最小的理论长宽比应为0.5:1。但由于底盘长宽比受行走轮直径、轮宽及重心的影响,底盘的合理长宽比值范围需趋近于理论长宽比。当机具作业宽幅大于等于机具轮宽时,可直接做倒U形转向;否则采用"4"和歪梨形组合掉头转向,实现地头宽度等于1个作业幅宽的转向。     

闭式脱粒滚筒的静动态性能分析

针对联合收割机中闭式脱粒滚筒有可能在外载荷作用下会发生较大变形和在外激励作用下发生共振的问题,采用SolidWorks软件对闭式脱粒滚筒进行了三维建模,以*.x_t格式导入Ansys Workbench建立有限元模型,然后对闭式脱粒滚筒进行静动态性能分析(即静态分析和模态分析)。静态分析结果表明,闭式脱粒滚筒的刚度和强度足够,变形均在设计允许范围之内;模态分析得到的闭式脱粒滚筒前6阶固有频率和振型结果表明,在规定的工况范围内,闭式脱粒滚筒在外激励作用下不会产生共振。研究结果为后续样机的设计和改进提供了理论依据。     

日光温室地埋管道温度场影响因素研究-基于Fluent

目前,越来越多的日光温室作业者通过在温室土壤中铺设热水循环地埋管道的方式来为温室夜间生产供热。为了了解温室地埋管道温度场的影响因素,运用GAMBIT建立土壤中不同直径的地埋管道二维网格模型,并采用Fluent软件模拟地埋管在冬季夜间环境下周围土壤温度场的变化。在网格模型中选取监测点,通过观测监测点温度了解埋管结构参数与土壤温度场的关系,为今后温室地埋管的埋设提供参考。     

离散元模拟外槽轮排肥器排量分析

排肥装置作为免耕播种机的重要组成部分,其排肥性能直接影响播种的出苗率、作物的长势及粮食的产量。为得到外槽轮排肥器不同槽轮工作长度的单位圆周排出质量和质量流率,本文采用离散元软件,对外槽轮排肥器转速为35r/min,槽轮工作长度为15、30、55mm时的排肥过程进行了模拟。模拟结果表明:外槽轮工作长度为15、30、55mm时,单位圆周排出质量分别为0.036 9、0.069 4、0.135 5kg/r;质量流率分别为0.0215、0.0405、0.0790kg/s。     

Canine fetal echocardiography: correlations for the analysis of cardiac dimensions

The aim of this study was to develop regression models for correlation of canine fetal heart development with body size to characterize normal development or suggest cardiac anomalies. Twenty clinically healthy pregnant bitches, either brachycephalic and non-brachycephalic, were examined ultrasonographically. Transabdominal fetal echocardiography was conducted every 4 days from the beginning of cardiac chambers differentiation until parturition. Ten cardiac parameters were measured: length, width and diameter of the heart; heart area; left and right ventricular dimensions; left and right atrial dimensions; and aortic and pulmonary artery diameter. Femoral length, biparietal diameter and abdominal cross-sectional area were also recorded. Regression equations were developed for each parameter of fetal body size, and linear and logarithmic models were compared. The model with the highest correlation coefficient was chosen to produce equations to calculate relative dimensions based on the correlations. Only the left-ventricular chamber differed between the two racial groups. Biparietal diameter was the independent parameter that produced the highest correlation coefficient for the most fetal cardiac dimensions, although good correlations were also observed using femoral length and abdominal cross-sectional area. Heart width and heart diameter were used as surrogates of cardiac development, as these measurements showed the best statistical correlation. Quantitative evaluation of fetal cardiac structures can be used to monitor normal and abnormal cardiac development.     

Tenogenic induction of equine mesenchymal stem cells by means of growth factors and low-level laser technology

Tendons regenerate poorly due to a dense extracellular matrix and low cellularity. Cellular therapies aim to improve tendon repair using mesenchymal stem cells and tenocytes; however, a current limitation is the low proliferative potential of tenocytes in cases of severe trauma. The purpose of this study was to develop a method useful in veterinary medicine to improve the differentiation of Peripheral Blood equine mesenchymal stem cells (PB-MSCs) into tenocytes. PB-MSCs were used to study the effects of the addition of some growth factors (GFs) as TGFβ3 (transforming growth factor), EGF2 (Epidermal growth factor), bFGF2 (Fibroblast growth factor) and IGF-1 (insulin-like growth factor) in presence or without Low Level Laser Technology (LLLT) on the mRNA expression levels of genes important in the tenogenic induction as Early Growth Response Protein-1 (EGR1), Tenascin (TNC) and Decorin (DCN). The singular addition of GFs did not show any influence on the mRNA expression of tenogenic genes whereas the specific combinations that arrested cell proliferation in favour of differentiation were the following: bFGF2 + TGFβ3 and bFGF2 + TGFβ3 + LLLT. Indeed, the supplement of bFGF2 and TGFβ3 significantly upregulated the expression of Early Growth Response Protein-1 and Decorin, while the use of LLLT induced a significant increase of Tenascin C levels. In conclusion, the present study might furnish significant suggestions for developing an efficient approach for tenocyte induction since the external administration of bFGF2 and TGFβ3, along with LLLT, influences the differentiation of PB-MSCs towards the tenogenic fate.